Neurological

Stroke Recovery: cell-therapy evidence and registered trials

A source-first research page for the exact condition. It does not recommend a cell product, clinic or private treatment.

Medical review statusPending clinical sign-offLast evidence update: 2026-08-05Methodology and editorial standards
Clinical review team: Dr Kamelia Milcheva, Hematologist · Dr Vadym Uvarov, Board-Certified Physician · Hepatobiliary Surgeon · Candidate of Medical SciencesEditorial responsibility: StemCellAtlas research teamEducational information only. This page does not provide medical advice, diagnosis or a treatment recommendation.

Registry snapshot

ClinicalTrials.gov returned 110 registered studies for the stored condition/intervention query, including 13 recruiting records, retrieved 2026-08-05T06:02:03+00:00. A registry count does not establish efficacy, approval, relevance or eligibility; inspect each study's design, product, status and inclusion criteria.

Research activity over time

Registration of new studies slowed: 25 newly registered studies in 2021–2025 against 32 in 2016–2020. The first study in this registry query was posted in 2005; the registry now holds 110 in total, of which 13 are recruiting. Counting is by first-posted date, so the series reflects when research was registered — not enrolment, completion or results.

Newly registered Stroke Recovery studies by year
20165
20179
20186
20197
20205
20215
20223
20236
20244
20257
20266

Source: ClinicalTrials.gov API v2, retrieved 2026-08-05. A registration count is not evidence of efficacy, approval or eligibility. Open the exact query ↗

What the trial registry actually shows

Our own count of every study registered on ClinicalTrials.gov for stroke with a stem-cell intervention, retrieved 2026-09-05. A registration is a declaration of intent, not a result — which is why the status column matters more than the total.

Status in the registryStudiesShare
Completed4036%
Status not updated by sponsor2926%
Recruiting now1211%
Withdrawn before enrolling98%
Not yet recruiting87%
Active, closed to entry44%
Terminated early33%
No longer available22%
Suspended22%
Enrolling by invitation only11%
All registered studies110100%

Reading it: 14 stopped before finishing — terminated, withdrawn or suspended, 13% of the total; 15 carry no assigned trial phase, meaning they sit outside the phased development path that leads to an approved medicine; 29 reached Phase 2 or later, against 66 still at Phase 1 or earlier; 29 have had no status update from the sponsor and may be dormant.

Which cell family is actually studied here

The same condition, split by the three families that registries can distinguish. Sub-types such as Muse, placental or fetal preparations are not separated in the registry and sit inside the mesenchymal count.

Mesenchymal stromal cells46Exosomes18Haematopoietic transplant14
Cell familyStudies
Mesenchymal stromal cells46
Exosomes18
Haematopoietic transplant14

Mesenchymal cells dominate the registered work here: 46 studies against 14 using haematopoietic transplant.

Counts are our own extraction from the ClinicalTrials.gov API, retrieved 2026-09-05. The query behind them is published with the dataset so anyone can repeat the count. Nothing here is evidence of benefit or a treatment recommendation.

What to verify before interpreting a study or offer

  1. The exact product, cell source, processing, dose and delivery route.
  2. The indication, study phase, comparator, endpoints, status and eligibility criteria.
  3. Whether the proposed use is authorised, part of a registered trial or otherwise investigational.
  4. Provider and manufacturing authorisations, release testing, traceability and adverse-event reporting.
  5. How the proposal compares with current standard care, reviewed by an independent physician.

Sources & further reading

Registry data is a discovery aid, not evidence that a treatment works or is suitable for an individual patient.

Compare cell-therapy evidence, registered studies and published price observations.

StemCellAtlas is a source-first research and cost-planning guide. It separates registry and regulator evidence from heterogeneous commercial observations.

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